Caricamento...
Phenotyping of Rare CFTR Mutations Reveals Distinct Trafficking and Functional Defects
Background. The most common CFTR mutation, F508del, presents with multiple cellular defects. However, the possible multiple defects caused by many rarer CFTR mutations are not well studied. We investigated four rare CFTR mutations E60K, G85E, E92K and A455E against well-characterized mutations, F508...
Salvato in:
| Pubblicato in: | Cells |
|---|---|
| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2020
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7140603/ https://ncbi.nlm.nih.gov/pubmed/32204475 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells9030754 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|